A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429077



Internal ID21086630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33888456..33969282hg38UCSC Ensembl
chr8:33745974..33826800hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3880827
hg1980827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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